1) brain drug delivery
![点击朗读](/dictall/images/read.gif)
脑药物转运
2) nose-brain transport
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药物经鼻-脑转运
1.
The in vitro model to study the direct nose-brain transport of drugs was built by using excised bovine olfactory mucosa and Franz diffusion chamber,with huperzine A and trybizine hydrochloride as the model drugs.
分离牛嗅黏膜,以石杉碱甲和盐酸锥双净为模型药物,用Franz扩散池,建立评价药物经鼻-脑转运的体外模型。
3) Drug transport
![点击朗读](/dictall/images/read.gif)
药物转运
1.
The role of organic anion transporting polypeptide in drug transport;
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有机阴离子转运肽在药物转运中的作用
2.
So the promotion of active drug transporting into the brain will become an important problem of waiting to be solved.
现代医学研究也日益认识到,除结构屏障外,由内皮细胞上药物转运体所构成的功能屏障在脑病治疗中也具有重要作用。
4) drug delivery
![点击朗读](/dictall/images/read.gif)
药物转运
1.
Sodium-coupled monocarboxylate transporters and their actions in drug delivery
![点击朗读](/dictall/images/read.gif)
Na~+偶联单羧酸转运蛋白及其在药物转运中的作用
2.
In order to construct a special brain drug delivery vector, the gene of single chain antibody (Ox26 ScFv) to rat transferrin receptor was synthesized by 18 fragments.
为构建特异性的脑药物转运载体 ,分段合成了抗大鼠转铁蛋白受体的单链抗体基因 (Ox2 6 scfv) 。
5) drug transporter
![点击朗读](/dictall/images/read.gif)
药物转运体
1.
Effects of drug transporters on the intestinal absorption of trans-resveratrol;
![点击朗读](/dictall/images/read.gif)
药物转运体在反式白藜芦醇肠道吸收中的作用
2.
However, its long-term application may induce or inhibit hepatic drug metabolic enzymes and drug transporters, which result in the alteration of drug metabolism and the occurrence of drug-drug interaction.
然而,大蒜长期应用,可能对肝脏药物代谢酶及体内药物转运体的活性产生诱导或抑制效应,从而引起自身或其他合用药物代谢的改变和导致药物相互作用的发生。
3.
This review is mainly concerned about the effects of drug transporters on drug excretion and the possibility in the development and clinical application of new drugs.
本文介绍了药物转运体在药物排泄过程中的作用,探讨了其在新药研发和临床应用中的可能性。
6) drug transporter
![点击朗读](/dictall/images/read.gif)
药物转运蛋白
1.
Research advances in drug transporters and multidrug resistance;
![点击朗读](/dictall/images/read.gif)
药物转运蛋白和多药耐药性的研究进展
2.
Aim:To compare the effects of the drug transporter substrates such as probenecid,methotrexate,digoxin and verapamil on renal excretion of dicycloplatin in rats.
目的:比较在大鼠中丙磺舒、甲氨蝶呤、地高辛、维拉帕米等不同药物转运蛋白底物对双环铂肾排泄的影响。
3.
Chapter 1 The polymorphisms of drug transporters on the effect of telmisartan pharmacokineticsBackgroundTelmisartan is an angiotensinⅡreceptor antagonist,can high selectively and irreversibly antagonize AT1 receptor,but don\'t inhibit the angiotensin-converting enzyme or affect the effects of bradykinin.
第一章药物转运蛋白基因的遗传多态性对替米沙坦药动学的影响研究背景替米沙坦(telmisartan)是一种血管紧张素Ⅱ(AngiontensinⅡ,AngⅡ)1型(AT1)受体拮抗药,具有高选择性、不可逆地拮抗AT_1受体,而不抑制血管紧张素转换酶,不影响缓激肽的效应;也不与其它激素受体和离子通道结合或产生阻断作用,因而不影响包括心血管调节在内的其它受体系统。
补充资料:和淮南李司空同转运员外(一作同转运卢员外
【诗文】:
层层高阁旧瀛洲,此地须征第一流。丞相近年萦倚望,
重才今日喜遨游。荣持健笔金黄贵,恨咽离筵管吹秋。
谁继伊皋送行句,梁王诗好郢人愁。
【注释】:
【出处】:
全唐诗:卷656-12
层层高阁旧瀛洲,此地须征第一流。丞相近年萦倚望,
重才今日喜遨游。荣持健笔金黄贵,恨咽离筵管吹秋。
谁继伊皋送行句,梁王诗好郢人愁。
【注释】:
【出处】:
全唐诗:卷656-12
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条